| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:68658673-68658888 | Common:2; Rare:40 | ||||
| chr16:68659723-68659793 | Rare:8 | ||||
| chr16:68738019-68738407 | Rare:93; Clinvar:11; Clinvar (benign):16 | ||||
| chr16:68750462-68750696 | Common:1; Rare:35 | ||||
| chr16:68756339-68756511 | Common:1; Rare:28 | ||||
| chr16:68759042-68759216 | Rare:23 | ||||
| chr16:68985941-68986264 | Rare:55 | ||||
| chr16:69040150-69040347 | Rare:34 | ||||
| chr16:69150589-69150810 | Rare:81 | ||||
| chr16:69599606-69599646 | Common:1; Rare:7 | ||||
| chr16:70014104-70014241 | Rare:15 | ||||
| chr16:70250233-70250282 | Common:1; Rare:9 | ||||
| chr16:70250330-70250382 | Rare:13 | ||||
| chr16:70419970-70420014 | Rare:14 | ||||
| chr16:70555506-70555656 | Rare:35 |